Pure Global

VISITC Lasik PVA Spears - Indonesia BPOM Medical Device Registration

VISITC Lasik PVA Spears is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203320412. The device is manufactured by BEAVER VISITEC INTERNATIONAL INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN INDEPENDENT MEDEQ.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
VISITC Lasik PVA Spears

VISITEC Lasik PVA Spears

Analysis ID: AKL 21203320412

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MAIN INDEPENDENT MEDEQ

AR Address

Ruko Graha Mas Pemuda Blok AC-19 jL. Pemuda Blok AC-19 Jl. Pemuda Kel. Jati Kec. Pulo Gadung Jakarta Timur

Registration Date

Oct 25, 2023

Expiry Date

Dec 31, 2026

Product Type

Surgical Eye Equipment

Ophthalmic sponge.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from BEAVER VISITEC INTERNATIONAL INC.
Products from the same manufacturer (2 products)